FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NON-RETENTION ENEMA SYSTEM
K Number: K781923
·
Decision Aug 3, 1979
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
39
Applicant Total
1
Review Days
260
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Basic Information
- Device Name
- NON-RETENTION ENEMA SYSTEM
- K Number
- K781923
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 876.5220
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Applicant
- Hudson Kendale Assoc., Inc.
- Date Received
- November 16, 1978
- Decision Date
- August 3, 1979
- Product Code
- KPL
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- GU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KPL | Colonic Irrigation System | FDA class 2 | Gastroenterology, Urology |
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